retinitis pigmentosa 37
retinitis pigmentosa that has material basis in mutation in the NR2E3 gene on chromosome 15q23
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retinitis pigmentosa 37
Summary
retinitis pigmentosa 37 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- retinitis pigmentosa 37's instance of is recorded as rare disease[3].
- retinitis pigmentosa 37's instance of is recorded as class of disease[4].
- retinitis pigmentosa 37 is a type of retinitis pigmentosa[5].
- retinitis pigmentosa 37 is a type of genetic disease[6].
- retinitis pigmentosa 37 is a type of autosomal dominant disease[7].
- retinitis pigmentosa 37 is a type of autosomal recessive disease[8].
- retinitis pigmentosa 37's genetic association is recorded as NR2E3[9].
- retinitis pigmentosa 37's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110399[10].
- retinitis pigmentosa 37's exact match is recorded as http://identifiers.org/doid/DOID:0110399[11].
- retinitis pigmentosa 37's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
retinitis pigmentosa 37 is known by 4 alternative names across languages and contexts.[2]